54653-25-7 Usage
Description
Ethyl-5-hexenoate is an organic compound known for its distinct fruity aroma. It is characterized by a sweet, pineapple, jamy overripe fruity, and strawberry scent with onenanthic tutti-fruitti candy nuances. Ethyl-5-hexenoate is reportedly present in tea, pineapple, strawberry, and Chinese quince peel, and its chemical properties contribute to its unique and pleasant smell.
Uses
Used in Flavor and Fragrance Industry:
Ethyl-5-hexenoate is used as a flavoring agent for its sweet, fruity, and pineapple-like aroma. Its taste threshold values range from 5 to 10 ppm, making it a suitable addition to the flavor industry to enhance the taste and aroma of various products.
Used in Aromatherapy:
Due to its pleasant and fruity scent, Ethyl-5-hexenoate can be used as an aromatherapy agent. Its odor characteristics at 10,000 ppm include a sharp estery, sweet with ripe fruity notes of pineapple, apple, and strawberry, along with winy and acidic depth notes. This makes it a potential candidate for creating a relaxing and uplifting atmosphere in aromatherapy applications.
Used in Perfumery:
Ethyl-5-hexenoate's unique and fruity aroma also makes it suitable for use in the perfumery industry. It can be used as a base note or blended with other fragrance components to create complex and long-lasting scents for perfumes and colognes.
Used in the Food and Beverage Industry:
The fruity and sweet characteristics of Ethyl-5-hexenoate make it an ideal additive for the food and beverage industry. It can be used to enhance the flavor and aroma of various products, such as fruit juices, candies, and baked goods, providing a more enjoyable and appetizing experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 54653-25-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,5 and 3 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 54653-25:
(7*5)+(6*4)+(5*6)+(4*5)+(3*3)+(2*2)+(1*5)=127
127 % 10 = 7
So 54653-25-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H14O2/c1-3-5-6-7-8(9)10-4-2/h3H,1,4-7H2,2H3
54653-25-7Relevant articles and documents
Microbiological transformations. Part 51: The first example of a dynamic kinetic resolution process applied to a microbiological Baeyer-Villiger oxidation
Berezina, Nathalie,Alphand, Veronique,Furstoss, Roland
, p. 1953 - 1955 (2002)
The dynamic resolution of racemic 2-benzyloxymethylcyclopentanone 1 upon microbiologically mediated Baeyer-Villiger oxidation allowed the corresponding (R)-lactone 2 to be prepared in 85% yield and 96% ee.
Sunlight oxidation of alkyl aryl tellurides to the corresponding carbonyl compounds: A new carbonyl precursor
Ouchi, Akihiko,Hyugano, Takeshi,Liu, Chuanxiang
supporting information; experimental part, p. 4870 - 4873 (2010/01/06)
Alkyl aryl tellurides were efficiently transformed to the corresponding carbonyl compounds by photo-oxidation with sunlight without affecting various functional groups in the alkyl moiety. The tellurides can be used as a new carbonyl precursor, and the photolysis can be conducted without special equipment for light sources.
Synthesis of unsaturated dibasic acid esters from five-, six-, and seven-membered cycloalkanones
Starostin,Furman,Ignatenko,Barkova,Nikishin
, p. 2016 - 2019 (2007/10/03)
A new route to diesters of symmetrical octene-, decene-, and dodecenedioic acids was proposed. The ratio of the cis/trans-isomers was 1:4. The synthesis involved oxidative splitting of five-, six-, and seven-membered cycloalkanones with hydrogen peroxide into the corresponding ω-alkenoic acids followed by esterification and metathesis over Re2O7/B 2O3-Al2O3-SnMe4.
